Allele Registry

Canonical Allele Identifier: PA2828120411

Gene: GFAP HGNC NCBI

ClinVar RCV:

RCV000056831

RCV000192170

ClinVar Variation:

66437

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350775.1:p.Glu371Gly	CA217115 NM_001363846.2:c.1112A>G